软骨
骨关节炎
类有机物
促炎细胞因子
阿格里坎
益生菌
细胞生物学
生物
医学
生物信息学
代谢组
平衡
发病机制
弹性蛋白
机械转化
计算生物学
机械反应
软骨细胞
关节软骨
细胞外基质
体内
肠道菌群
化学
信号转导
软骨发生
病理
II型胶原
炎症
作者
Jun Liu,Ning Zhang,Yiting Lei,Xiaoshuai Wang,Xiang Zhang,Wei Huang,Changhai Ding,Denghui Xie,Jun Qing Yu,Rocky S. Tuan,Zhong Alan Li
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-10-09
卷期号:12 (41): eaeg8557-eaeg8557
标识
DOI:10.1126/sciadv.aeg8557
摘要
Although emerging evidence implicates gut microbiome-cartilage cross-talk in the pathogenesis of osteoarthritis (OA), the most common joint disease, studying this microbe-gut-joint axis remains challenging due to limitations of animal models and conventional in vitro systems. Here, we report a microbe-gut-cartilage axis-on-a-chip (MGCAoC) that recreates tissue-specific microenvironments with oxygen gradients and physiological fluid shear. The computer simulation-optimized chip design generates an anoxic-oxic interface for the gut module and enables perfusion of probiotic metabolites to human cartilage organoids without cross-contamination. Multiomics profiling suggested that probiotic metabolites may promote cartilage anabolism, potentially involving PI3K and MAPK pathway, and this effect was associated with up-regulated collagen type II and aggrecan expression while suppressing metalloproteinases. In inflamed cartilage organoids, these metabolites were associated with reduced proinflammatory signaling while preserving matrix integrity. The chondroprotective effects were confirmed using cartilage organoids derived from patients with OA treated with identified metabolites. This MGCAoC enables mechanistic investigation of gut-joint axis physiology and provides a versatile preclinical tool for screening probiotic-based OA therapeutics.
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